苯基 N-(2,4,6-三甲基苯基)氨基甲酸酯

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: Using n-pentylamine (304.2 mg), triethylamine (442.2 mg), [[2′-(N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl] bromide (400 mg) and phenyl 2,4,6-trimethylphenylcarbamate (233.8 mg), N′-pentyl-N-(2,4,6-trimethylphenyl)-N′-[[2′-[N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl]urea (113 mg) was obtained by a similar procedure as in Example 1. Yield: 22%.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: Using n-pentylamine (304.2 mg), triethylamine (442.2 mg), [[2′-(N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl] bromide (400 mg) and phenyl 2,4,6-trimethylphenylcarbamate (233.8 mg), N′-pentyl-N-(2,4,6-trimethylphenyl)-N′-[[2′-[N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl]urea (113 mg) was obtained by a similar procedure as in Example 1. Yield: 22%.